Veenman C L
Institute of Toxicology, Swiss Federal Institute of Technology, Schwerzenbach, Switzerland.
Eur J Morphol. 1997 Oct;35(4):220-33. doi: 10.1076/ejom.35.4.220.13079.
This paper reviews the organization of the avian and mammalian striatum. The striatum receives input from virtually the entire rostrocaudal and mediolateral expanse of the cerebral cortex. The corticostriatal projections appear to be glutamatergic, forming excitatory synapses in the striatum. Another major projection to the avian striatum that also appears to be glutamatergic stems from a set of nuclei in the dorsal zone of the avian thalamus that are comparable to the mammalian intralaminar, mediodorsal, and midline nuclei. Furthermore, the striatum receives a massive projection from dopaminergic neurons of the ventral tegmental area and substantia nigra in the midbrain tegmentum. In return, the midbrain tegmentum receives a direct GABAergic/substance P-ergic/ dynorphinergic projection from the striatum, as well as an indirect one formed by GABAergic/substance P-ergic/ dynorphinergic and GABA-ergic/enkephalinergic striatal neurons projecting to the pallidum in the first step, and pallidal GABAergic/LANT6/parvalbumin neurons projecting to the midbrain tegmentum in the second step. In addition to its projection neurons, the striatum possesses GABAergic and cholinergic interneurons. One motor output pathway of the striatum runs via the pallidum and dorsal thalamic ventral tier nulei to the motor cortex. In addition to this pathway, birds possess a major descending pathway from the basal ganglia to the tectum via the GABAergic nucleus spiriformis lateralis in the pretectum. On hodological and topological grounds, similar nuclei, although not GABAergic, can be found in mammals. Finally, an other striatal motor output is formed by a sequential GABAergic pathway from the basal ganglia via the substantia nigra to the tectum. In conclusion, it appears that the organization of the avian and mammalian basal ganglia is similar rather than different.
本文综述了鸟类和哺乳动物纹状体的组织结构。纹状体几乎接收来自大脑皮质整个前后和内外侧区域的输入。皮质-纹状体投射似乎是谷氨酸能的,在纹状体内形成兴奋性突触。另一个投射到鸟类纹状体的主要通路似乎也是谷氨酸能的,它起源于鸟类丘脑背侧区的一组核团,这些核团与哺乳动物的板内核、背内侧核和中线核相当。此外,纹状体接收来自中脑被盖腹侧被盖区和黑质多巴胺能神经元的大量投射。作为回报,中脑被盖接收来自纹状体的直接γ-氨基丁酸能/ P物质能/强啡肽能投射,以及由γ-氨基丁酸能/ P物质能/强啡肽能和γ-氨基丁酸能/脑啡肽能纹状体神经元首先投射到苍白球,然后苍白球γ-氨基丁酸能/LANT6/小白蛋白神经元投射到中脑被盖形成的间接投射。除了其投射神经元外,纹状体还拥有γ-氨基丁酸能和胆碱能中间神经元。纹状体的一条运动输出通路通过苍白球和丘脑背侧腹层核到达运动皮质。除了这条通路外,鸟类还拥有一条从基底神经节经顶盖前区外侧螺旋状核到顶盖的主要下行通路。基于神经束路学和拓扑学的原因,在哺乳动物中可以发现类似的核团,尽管它们不是γ-氨基丁酸能的。最后,纹状体的另一条运动输出是由一条从基底神经节经黑质到顶盖的连续γ-氨基丁酸能通路形成的。总之,鸟类和哺乳动物基底神经节的组织结构似乎是相似而非不同的。